Urea condensate salt of sulfur oxyacid for fire control

ABSTRACT

Aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid and/or aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid composition may be utilized to fight grass, forest, building fires, and flame retard other flammable organic material by applying it on or incorporating it in these flammable organic materials. The aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid and/or aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid composition may be incorporated into flammable materials such as solid and foam plastic and natural materials. Nitrogen containing compound urea condensate salts of sulfur oxyacid or it&#39;s composition are produced by mixing and reacting urea and a nitrogen containing compound with sulfur oxyacids and it&#39;s composition is produce by adding and mixing carbonization auxiliaries, such as phosphorus containing compounds, metal containing compounds that will accelerate carbonization, heat reflector, surfactant and fillers to the aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid.

This application is a continuation in part of patent application Ser. No. 09/149,847 filed Sep. 8, 1998 now U.S. Pat. No 6,258,298 which is a division of patent application Ser. No. 08/723,779 filed Aug. 30, 1996, now U.S. Pat. No. 5,854,309.

FIELD

This invention concerns nitrogen containing compound urea condensate salt of sulfur oxyacid as fire controlling agent. The invention also concerns the preparation and use of nitrogen containing compound urea condensate salt of sulfur oxyacid. The nitrogen containing compound urea condensate salt of sulfur oxyacid and/or its composition is useful to stop house fires, grass and forest fires, to produce flame retarded water based plastic, flame retarded plastics, flame retardant polyurethane foam, etc, and fire retardant flammable organic materials by spraying the outside with aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid and/or its composition.

BACKGROUND

Urea in the form of a solid compound has been used as a flame retardant agent in polyurethane foams as outline in U.S. Pat. No. 4,385,131 (Fracalossi, et al.). Many patents use solid urea condensates, urea phosphates, urea borates and urea derivative as the flame retardant agent. The use of aqueous or powdered nitrogen containing compound urea condensate salt of sulfur oxyacid as the fire retardant compound is novel. When solid urea is used in sufficient amounts, as the flame retardant retardant compound in the production of flame retardant organic products, such as polyurethane products it leaves a slimy or soapy feel to the outer surface of the urethane products, which is very undesirable. The urea migrates out and the product becomes less fire retardant. When the powdered or aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid is utilized, it reacts with the polyisocyanate and becomes a part of the product. There is no slimy or soapy feel to this foam. Aqueous ammonium urea condensate salt of sulfur oxyacid may be used as a fertilizer and is very environmentally safe product to use on grass and forest fires. When used for fire fighting the aqueous ammonium urea condensate salt of sulfur oxyacid may contain coloring agents such as iron oxide, thickening agents, gelling agents, corrosive inhibitors, bactericide agents, surfactant and wetting agents. Aqueous ammonium urea condensate salt of sulfur oxyacid is more economical to use to fight fires than the commonly used fire fighting chemicals such as various ammonium phosphates and ammonium sulfate.

What is lacking and what is needed are useful, safe and inexpensive flame retardant compounds found in aqueous or powdered nitrogen containing compound urea condensate salt of sulfur oxyacid. What is additionally lacking are compositions have aqueous or powdered nitrogen containing compound urea condensate salt of sulfur oxyacid employed therein.

SUMMARY

In one aspect, the invention comprises the fire retardant aqueous or powdered nitrogen containing compound urea condensate salt of sulfur oxyacid. Another aspect of the invention is a process to prepare the aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid composition.

Another aspect of this invention is the process to prepare an aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid or composition by mixing:

(A) urea, in the amount of 25 to 200 parts by weight;

(B) nitrogen containing compound that will react with sulfur oxyacid or urea, in the amount of 1 to 200 parts by weight;

(C) sulfur oxyacid and/or it's salts, in the amount of 5 to 50 parts by weight;

(D) carbonization auxiliaries, in the amount of 0 to 300 parts by weight;

(E) metal containing compound that will accelerate the carbonization process, in the amount of 0 to 30 parts by weight;

(F) heat reflecting compound, in the amount of 0 to 30 parts by weight;

(G) filler, in the amount of 0 to 300 parts by weight;

(H) surfactant, in the amount of 0 to 30 parts by weight;

(I) water, in the amount of 0 to 500 parts by weight.

Another aspect of this invention is to apply on and/or incorporating in a more flammable organic material (Component J) the flame retardant compounds, aqueous or sold nitrogen containing compound urea condensate salt of sulfur acid and/or composition.

Another aspect of this invention is to utilize the aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid and/or the aqueous nitrogen containing compound urea condensate acid salt of sulfur oxyacid composition to fight fires such as grass fires, forest fires, house fires, furniture fires, etc. In fighting grass fires a water diluted solution of aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid and/or aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid composition, preferable ammonium urea condensate salt of sulfur oxyacid, with or without, surfactant, to produce bubbles, may be sprayed directly on the flames or may be sprayed in front of the flames thereby wetting the organic materials in front of the fire. The aqueous ammonium urea condensate salt of sulfur oxyacid and/or aqueous ammonium urea condensate salt of sulfur oxyacid composition, even after drying, and for several day afterwards, will prevent the coated organic materials such as grass, leaves and bushes from catching on fire when exposed to flames. Some of the ammonium urea condensate salt of sulfur oxyacid is absorbed by the grasses, leave, limbs, fir needles, etc. thereby making dry plants flame retardant.

Component A

Any suitable aqueous urea or solid urea may be utilized in this invention. The aqueous urea produced in the manufacturing process of producing urea and/or the aqueous urea produced by adding solid urea to water. Usually the aqueous solution of urea contains 50% or less of urea. Solid urea is preferred in the amount of 25 to 200 parts by weight. Urea condensate may also be used.

Component B

Any suitable nitrogen containing compounds that will react with a sulfur oxyacid compound or urea may be used in this invention. Aqueous and/or gaseous salt forming nitrogen compounds may be use, such as gaseous ammonia. Any suitable nitrogen containing compound, especially those containing reactive —NH₂, —COOH, —OH, —NCO, and/or epoxide radical, that will react with sulfur oxyacids and/or isocyanic acid and/or cyanic acid which is produced by heating urea may be utilized in this invention. The nitrogen containing compound may be an organic or an inorganic compound. Suitable organic nitrogen containing compounds may be an aliphatic, aromatic, cyclic, aliphatic-aromatic or aliphatic-cyclic compound such as, but not limited to, urea, urea derivatives for example, O-alkylureas, amino compounds, for example, melamine, melamine cyanurate, dicyandiamide, biuret, biuret-metal complex, cyanuric acid, cyamelide, guanidine, cyanoguanidine and aminoguanidine, ammonium carbonate, alkyl carbamates, alkyl isocyanates, polyisocyanates, sulfamic acid, ammonium sulfamate, amines, polyamines, thioureas, alkylanolamine, polyamides with free NH₂— radicals, amidines, amides, aldimines, ketimines, guanidine carbonate, amino carbonates, aminoborates, amino sulfates, thiourea, thiourea derivatives, compounds with active NH₂— radicals, such as amino phosphate, amino salts of organic phosphorus compounds and amino condensation salt of inorganic and organic phosphorus compounds containing active NH₂— radicals and mixtures thereof. The amino compounds and ammonia are the preferred nitrogen containing compound. The nitrogen containing compound may be utilized in the amount of 1 to 200 parts by weight. Aqueous ammonia is preferred. Ammonia may be utilized in the amount necessary to adjust the pH to the desired pH. Ammonia is also produced by the condensation of urea when heated.

Component C

Any suitable sulfur oxyacid or it's salts that will react with urea may be used, such as sulfurous acid, sulfuric acid, pyrosulfuric acid, ammonium sulfate, ammonium hydrogen sulfate, ammonium sulfite, ammonium thiosulfate, urea hydrogen sulfate, urea sulfate, melamine hydrogen sulfate, amino hydrogen sulfates, biuret sulfate, lignin sulfate, lignin sulfite, amine hydrogen sulfates, polyamine hydrogen sulfates, metal hydrogen sulfates, alkyl hydrogen sulfates, aryl hydrogen sulfates and mixtures therof. Sulfuric acid, dilute or concentrated, is preferred acid. Ammonium sulfate or ammonium hydrogen sulfate is the preferred sulfur oxyacid salt. The sulfur oxyacid is utilized in the amount of 5 to 50 parts by weight.

Component D

Any suitable carbonization auxiliaries may be utilized in this invention. Suitable carbonization auxiliaries are compounds that in the presence of fire assist the formation of a carbonization foam or char, such as, additives that produce acidic components in the pyrolysis mixture, such as phosphorus acids, boric acids or sulfuric acids. These acidic components are compounds such, for example, acids or salts, or their derivatives of sulfur, boron and phosphorus, such as, boron-phosphates, silicon-phosphorus compounds, phosphates, and polyphosphates of ammonia, amines, polyamines, amino compounds, thioureas and alkyanolamines, but boric acid and its salts and their derivatives, organic phosphorus compounds and their salts, halogenated organic phosphorus compounds, their salts and their derivatives, sulfuric acids, their salts and their derivatives such as ammonium sulfate, urea sulfate, etc., may also be used for this purpose. The commonly known fertilizer which contains phosphorus or sulfur are inexpensive carbonization auxiliaries that can be used with the aqueous ammonium urea condensate salt of sulfuric acid, especially in fire fighting and fire prevention and are preferred. The carbonization auxiliaries and other flame retardant agents may be used in quantities of 0 to 300 parts by weight. The carbonization auxiliaries and other flame retardant agents are not a necessary component but when used is used in an amount of 5 to 200 part by weight. The ammonium phosphates may also act as a corrosive inhibitor.

The nitrogen containing salts of phosphorus acids are the preferred carbonization compounds, such as amino phosphate, amine and polyamine phosphates, amino salts of organic phosphorus compounds and amino condensation salt of inorganic and organic phosphorus compounds. The condensation salt of phosphorus compounds are produced by contacting urea condensates such as, biuret, cyanuric acid and cyamelide or other amino compounds with a phosphorus containing compound that will react with an amino compound, under conditions sufficient to prepare an amino salts of a phosphorus containing compound. Suitable inorganic phosphorus compounds include, but not limited to, phosphoric acid, pyrophosphoric acid, triphosphoric acid, metaphosphoric acid, phosphorous acid, hydrophosphorous acid, phosphinic acid, phosphinous acid, phosphine oxide, phosphorus trihalides, phosphorus oxyhalides, phosphorus oxide, and their salts, amino phosphates, amine phosphates, mono-metal hydrogen phosphates, ammonium dihydrogen phosphate, ammonium phosphate, bromated phosphates, alkali metal dihydrogen phosphate, and halogenated phosphate-phosphite and their halides and acids. organic phosphorus compounds include, but not limited to, alkyl, cyclic, aryl and alkyl-aryl phosphorus compounds, such as, alkylchlorophosphines, alkyl phosphines, alkyl phosphites, dialkyl hydrogen phosphites, dialkyl alkyl phosphonates, trialkyl phosphites, organic acid phosphates, organic diphosphonate esters, aryl phosphites, aryl hydrogen phosphates, halogenated phosphonates esters, biuret phosphate, cyanuric phosphate, cyamelide phosphate, and urea, biuret, cyanuric acid and cyamelide borates and mixtures thereof.

Component E

Any suitable metal-containing compound that will accelerate carbonization effect used in this invention increases the amount of carbonization residue after combustion, thereby enhancing the flame retardant effect and may be used in this invention. These compounds include, but not limited to, alkaline earth metal borates such as magnesium borate, calcium magnesium borate and the like, manganese borate, zinc borate, metal oxides of titanium oxide, tin oxide, nickel oxide, zinc oxide and the like, ferrocene, dimethylglyoxime copper, acetyl-acetonatocooper, hydroxyquinoline nickel and the like, zinc thiocarbamate compounds such as zinc dimethylthio-carbamate, zinc di-n-butyldithiocarbamate and the like, mercaptobenzothiazole zinc compounds such as mercaptobenzothiazole zinc and the like, salicyadehyde zinc compounds such as salicylaldehyde zinc and the like, metal hydroxides such as aluminum hydroxide, magnesium hydroxide, calcium magnesium hydroxide, zirconium hydroxide and the like and mixtures thereof. The most preferable compounds are selected from zinc oxide, zinc thiocarbamates, the mercaptobenzothiazole zinc compounds the salicyaldehyde zinc compounds, zinc borate and the alkaline earth metal borates. The are utilized in the amount of 0 to 30 parts by weight. These metal containing carbonization accelerators are not necessary components but when used it is used in the amount of 1 to 30 parts by weight.

Component F

Any suitable compound that will reflect heat compound such as titanium oxide may be used in this invention and used in the amount of 0 to 30 part by weight.

Component G

Any suitable filler may be used in this invention. The fillers that may be utilized in the flame retardant mixture may be insoluble in the reaction mixtures. They may be inorganic substances, such as, alkali metal silicates, alkaline earth metal silicates, metal silicates, silica, metals, oxides, carbonates, sulfates, phosphates, borates, glass beads or hollow glass beads. Hydrated aluminum oxide is preferred. They may be organic substances, such as, amino compounds, such as urea, melamine, dicyandiamide, urea condensates, urea-amino condensates, partially hydrolyzed urea condensates and other amino derivatives or their formaldehyde resins, amino phosphates, amino salts of organic phosphates, phenol-aldehyde resin powder, ammonium sulfates, urea sulfates, biuret sulfate, nitrogen containing sulfates, powdered coke, graphite, graphite compounds, Portland cement, lignin, lignin sulfate, lignin sulfite and mixtures thereof. The organic halide flame retardant compounds may also be added as fillers. The filler may be used in the amount of 0 to 300 parts by weight. Fillers are not a necessary component, but useful, and if used is used in the amount of 5 to 300 parts by weight.

Component H

Any suitable surfactant that will assist in the production of bubbles or used as a wetting agent may be used in this invention, such as soaps, detergents and silicon surfactants, such as water-soluble polyester siloxanes. Any surface active agent that will assist in the formation of foam or as a wetting agent such as cationic, anionic, non-ionic and amphoteric surfactants may be used in this invention. The surfactant may be used in the amount of 0 to 30 parts by weight. The surfactant is not a necessary component except when bubbles and wetting agents are desired, then it is used in the amount of 1 to 30 parts by weight.

Component J

Water may be added to the reactants or may be added to the nitrogen containing compound urea condensate salt of sulfur oxyacid or its composition to produce aqueous solutions or to react with the urea condensate or the nitrogen containing compound urea condensate salt of sulfur oxyacid. Water may be added in any suitable amount but usually in the amount of 0 to 500 parts by weight. Water is found in some of the sulfur oxyacid and in aqueous ammonia.

Component K

Any suitable organic material which is more flammable than the aqueous or solid nitrogen containing compound urea and/or it's composition may be used in this invention. Any suitable plastic resin composition or mixtures thereof and any suitable natural organic material maybe used in this invention and mixtures thereof. These materials may be in the form of a solid, cellular suspension, emulsion or solution but the plastic are preferable to be in the form of or a suspension, emulsion, solution or as a liquid monomer. Suitable plastic resin include, but not limited to, vinyl dienes, vinyl-diene copolymers, polyesters, polyester resins, phenoplasts, aminoplasts, polyepoxy resins, polyurethanes, furans, polyamides, polyimides, polycarbonates, homopolymers of such olefins as ethylene, propylene, and butylene; block copolymers, consisting of optional combination of these olefins; polymers of vinyl compounds such as vinyl chloride, acrylonitrile, methyl acrylates, vinyl acetates and styrene; copolymers of the foregoing olefins with vinyl monomers, copolymers and terpolymers of the foregoing olefins, with diene compounds; polyesters such as polyethylene terephthalate, polyester resins; polyamides such as nylon; polycarbonates, polyoxymethylene, silicones, polyethers, thioplasts, polytetrafluoroethylene, polysulfones, vinylidene, poly(vinyl acet compounds, cyclic unsaturated compounds, urethane-epoxy resins, polyimides, urethane silicates, cellulose nitrate rayon, regenerated cellulose film cellulose acetate, cellulose esters, cellulose ethers, cyanoethyl cellulose, chlorinated rubber and mixtures thereof.

Suitable natural products include but not limited to grass, weeds, leaves, wood, cellulose, lignin-cellulose, paper, cotton, wool, linen, dammars, copols, other natural resins, rosins, lignin, lignin sulfate, lignin sulfite, natural rubber, natural proteins, e.g., soya bean protein, silk, glues, gelatin, etc.; modified cellulose and mixtures thereof. Natural organic material and plastics may be mixed together. The nitrogen containing compound urea condensate salt of sulfur oxyacid and/or the nitrogen containing compound urea condensate salt of sulfur oxyacid composition, maybe utilized in the amount of 3-200 percent, percentage based on the weight of the more flammable organic material.

Any suitable polyisocyanate may be used in this invention organic polyisocyanates are preferred. The commercial available ones are preferred such as tolylene-2,4-diisocyanate, tolylene-2,6-diisocyanate, polymethylene polyphenyl isocyanate, diphenylmethane 4,4′-diisocyanate, 3-methlydiphenyl-methane-4,4′-diisocyanate, m- and p-phenylenediisocyanante, polyphenylpolymethylene isocyanates obtained by phosgenation, commercially known as “crude MDI”, modified polyisacyanates and mixtures thereof. Suitable organic polyisocyanates are exemplified by the organic diisocyanate which are compounds of the general formula

O═C═N—R—N—C═O

wherein R is a divalent organic radical such as an alkylene, aralkylene or arylene radical. Such radical may contain 2 to 20 carbon atoms. Any suitable compound with active hydrogens may be reacted with the polyisocyanates to produce polyurethane products. The preferred compound with active hydrogens are polyols. Polyurethane catalyst, blowing agents, surfactants, foam stabilizers, dyestuff, plasticizers, propellant, desiccant and fillers may also be used. Polyisocyanate which has the formula

Q(NCO)_(m)

in which m represent a number from 2 to 4 and Q represents an aliphatic hydrocarbon radical having 2 to 18 C atoms, a cycloaliphatic hydrocarbon radical having 4 to 15 C atoms, an aromatic hydrocarbon radical having 6 to 15 C atoms, or araliphatic hydrocarbon radical having 8 to 15 C atoms, in the amount of 25 to 100 parts by weight, and an organic compounds with 1 or more active hydrogens which will react with an isocyanate, in the amount of 25 to 100 parts by weight, containing a urethane catalyst, in the amount of 0.25 to 10 parts by weight, a plasticizer, propellants and a silicone surfactant, in the amount of 0.5 to 5 parts by weight, may be used as the flammable organic material. Any suitable polyepoxy compounds may be used in this invention such as ally glycidyl ether, tert-butyl glycidyl, and the like.

ILLUSTRATIVE EMBODIMENTS

In general, the urea and/or aqueous urea are usually produced by reacting ammonia and carbon dioxide in an aqueous medium while under heat and pressure. This aqueous urea may be utilized in this invention or the urea can be crystalized by removing some of the water. The solid urea may then be added to water to form an aqueous solution of urea which usually contains less than 50% urea. The aqueous urea may be heated to about its boiling point to produce urea condensates which are soluble in water or the urea heated to or above the melting point to produce a urea condensate such as biuret, cyanuric acid and cyamelide or a partially hydrolysed urea condensate. Ammonia is produced by heating urea to produce the urea condensate.

Any amount suitable amount of the aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid and/or it's composition, which may include carbonization auxiliaries, metal containing compounds that accelerated carbonization, heat reflecting substances, surfactant and fillers may be used to flame retard organic material. Preferably, when the nitrogen containing compound urea condensate salt of sulfur oxyacid and/or composition is incorporated in the more flammable organic material an amount of 3 to 200% by weight, percentage based on the weight of the more flammable organic material, is utilized. When the aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid and/or aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid composition is applied on the more flammable organic material, in a sufficient amount, will produce a less flammable organic material. Usually an amount that will wet the surface of the flammable organic material is sufficient.

The aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid and/or aqueous solid ammonium urea condensate salt of sulfur oxyacid composition is usually added on or incorporated in the flammable organic material at ambient temperature and pressure but elevated temperatures and pressure may be utilized when necessary.

The nitrogen containing compound urea condensate salt of sulfur oxyacid may be produced by mixing sulfuric acid and urea. The reaction is exothermic and heats up the mixture, then when urea is heated it reacts with itself to produce condensates such as biuret, cyanuric acid and cyamelide. Ammonia is produced in the condensate reaction. The ammonium urea condensate salt of sulfur oxyacid may also be produced by reacting aqueous ammonium, urea and sulfur oxyacid or by first reacting the ammonia with sulfur oxyacid to produce ammonium sulfur oxyacid then reacting it with urea or urea condensate or partially hydrolyzed urea condensate. These chemical reactions may take place at ambient or elevated temperature sufficient to melt the urea ranging from ambient to 180° C.

One method to measure this flame retardant capability is an oxygen index test. By selecting the various combinations of the mixture of nitrogen containing compound urea or it's compositions, which is then incorporate into a more flammable organic material, so that the average limiting oxygen index (LOI) can be raised 10 to 30 percent or more when compared to otherwise comparable samples without the flame retardant nitrogen containing compound urea composition. For example the LOI of three flexible polyurethane foams with the aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid composition were raised more than 30 percent to a LOI of 31.7, 30.3 and 30.7.

When the aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid and/or aqueous or solid nitrogen containing compound urea condensate salt of sulfur oxyacid composition was incorporated into rigid polyurethane foam and tested, with a propane torch with a 2″ flame held against the foam for one minute, the flame did not spread, the foam melted and/or a char was formed. The flame went out when the torch was removed. Various aqueous or solid nitrogen containing compound urea condensate salts of sulfur oxyacid compositions were incorporated into liquid resins then cured into a solid in the form of a ⅛×2″×6″ sample, for example, flexible polyepoxy resins, rigid polyepoxy resins, polyester laminating and flexible resin, polystyrene resin, polymethyl methyl acrylate resin, polyvinyl acetate resin, polyurethane, polyisoprene, polyethylene, acrylonitrile, etc, then tested with a propane torch having a 2″ flame, and held against the sample for 30 seconds. The flame did not spread, and went out when the flame was removed. Various mixture of aqueous nitrogen containing compound urea condensate salt of sulfur oxyacid and/or it's aqueous compositions was add to aqueous emulsions and organic solutions of the above plastics, then dried to form a test sample, then tested as above with good results.

The flexible flame retardant polyurethane foams were tested and passed the Calif. TB 133 test which utilizes a 100 gms of wood in the form of a crib being burned on top of the flexible foam. If more than 60 gms of the foam bums away it fails this test.

Various natural products such as wood shingles, paper, cotton cloth, and cardboard were coated with various aqueous solutions containing 30% nitrogen containing compound urea condensate salt of sulfur oxyacid or it's compositions with or without adhesives. Then after the product had dried, they were tested by applying a 2″ flame from a propane torch against the products, and the flame did not spread whereas the non coated products caught on fire and burned.

DESCRIPTION OF PREFERRED EXAMPLES

The present invention will now be explained herein-after by way of a few examples and comparative examples, these examples setting, however, no limits to this invention. Parts and percentage are by weight, unless otherwise indicated.

Example 1

Two-three heated moles of ammonia to one mol of heated carbon dioxide, heated at 160° to 210° C. is forced through a reactor which has an aqueous solution or oil-water slurry of ammonia and carbon dioxide which is being circulated at 160° to 210° C. and under 2-6000 psi to form ammonium carbamate which when heated lose 1 mol of water thereby producing a heated aqueous solution containing 60 to 80% urea, then 1 mole of sulfuric acid is added to 4 moles of the aqueous solution of urea thereby producing an ammonium urea condensate salt of sulfuric acid and some urea sulfate and biuret sulfate. The aqueous urea contains smaller amounts of ammonia, ammonium carbonate and biuret.

Example 2

Example 1 is modified wherein the aqueous urea is further processed wherein water is removed under low temperature and the urea crystalizes out. The powdered urea is then added to sulfuric acid, heated to 100 for 5 minutes thereby producing ammonium urea condensate salt of sulfuric acid. The reaction is exothermic.

Example 3

An area 3′×6′ with dry grass, weeds and leaves of an average of 1′ tall was sprayed in the middle 2′×3′ area with an aqueous solution containing 30% ammonium urea condensate salt of sulfuric acid, produced in example 1, until the grass and weeds were wet. One side of the dry untreated material was set on fire and the fire traveled to the center treated area and stopped. The other untreated area did not catch on fire.

Example 4

Example 3 is modified to wherein the wetted area was dried, and the other untreated side was set on fire. The fire traveled to the treated middle section then went out.

Example 5

Example 4 is modified wherein the middle section was dried for 4 days then a 3′ square pile of dry grass, weeds and leaves were placed next to the treated section on both sides then one side was set on fire. The fire burned to the treated section then some of the lower grass burned but went out before spreading to the other side.

Example 6

A 3′×3′×3′ pile of green fir tree branches was sprayed with a 30% aqueous solution of ammonium urea condensate salt of sulfuric acid until it was wet. A 2′×3′×2′ pile of dry grass was place on one side of the treated fir branches. The grass was set on fire and burned. A few needles of the fir branches next to the fire burned but did not spread to the rest of the branches. After the fir branches had dried another 2′×3′×2′ pile of dry grass was placed on the opposite side and next to the treated fir branches. The grass burned and some of the fir needles burned but the flames did not spread to the rest of the fir branches.

Example 7

A 1′×1′×5″ square of an untreated polyurethane foamed mattress was sprayed with an aqueous urea solution containing 25% ammonia urea condensate salt of sulfuric acid, produced in example 1, until the mattress foam was wet. The mattress was allowed to dry for 2 days then a burning cigarette was placed on the foam. The cigarette burned out but the foam did not catch on fire.

Example 8

Example 7 is modified wherein strips of cotton, polyester, nylon and acrylic cloth was placed on the treated polyurethane foamed mattress then the strips were set on fire. The cloth strip burned but the foam did not catch on fire.

Example 9

A 1′×1′×6″ rigid polyurethane foam was sprayed with an aqueous solution containing 20% ammonium urea condensate salt of sulfuric acid, produced in example 1, and 10% by weight of a carbonization auxiliary, ammonium polyphosphate until the foam was wet. The foam was dried for 3 days then flame tested by burning 50 gms of wood chips on top of the rigid foam. The foam did not catch on fire but there was about a 10% weight loss.

Example 10

Example 9 is modified wherein another carbonization auxiliary is used in place of ammonium polyphosphate and selected from the list below:

a) pyrophosphoric acid

b) phosphinic acid

c) phosphorus trichloride

d) phosphorus oxytrichloride

e) phosphorus oxide

f) ammonium dihydrogen phosphate

g) mono-aluminum phosphate

h) dimethyl methyl phosphonate (DMMP)

i) dimethyl hydrogen phosphite

m) phosphorus thiochloride

j) phenyl acid phosphate

k) methylchlorophosphine

l) phosphorus

n) tris(2-chloropropyl) phosphate

o) triphenyl phosphite

p) tris 2-chloroethyl phosphite

q) triethyl phosphite

r) urea dihydrogen phosphate

s) diethyl phosphite

t) trimethyl phosphite

u) dibutyl pyrophosphoric acid

v) O,O-dimethyl hydrogen dithiophosphate

w) melamine hydrogen boron-phosphate

x) hypophosphorous acid

y) methyl amine salt of phosphoric acid

z) ammonium sulfate

Example 11

A 4′×4′×3′ pile of dry branches from fir, cedar and oak trees was set on fire, then after the fire was burning good it was sprayed with an aqueous solution containing 20% by weight of ammonium urea condensate salt of sulfuric acid, produced in example 2, and the fire went out quickly.

Example 12

Example 9 is modified wherein another carbonization auxiliary is used in place of ammonium polyphosphate and selected from the list below:

a) dimelamine phosphate

b) dicyandiamide phosphate

c) urea dihydrogen phosphate

d) guanidine phosphate

e) aminoguanidine phosphate

f) diethyltriamine urea phosphate

g) melamine salt of dimethyl methyl phosphonate

h) melamine salt of dimethyl hydrogen phosphite phosphite

i) methylamine melamine phosphoric acid

j) methyl carbamate salt of phosphoric acid phosphate

k) melamine salt of boron-hydrogen phosphate

l) O-methyl urea

m) urea salt of boron-phosphate

n) urea-formaldehyde phosphate

o) aminophenol phosphate

p) ammonium urea phosphate

q) ammonium melamine phosphate

r) melamine salt of trimethyl

s) melamine salt of phenyl acid

t) cyanuric phosphate

Example 13

About 25 parts by weight of aqueous solution containing 75% ammonium urea condensate salt of sulfuric acid of example 1, 20% sucrose, 2% amine urethane catalyst and 0.3% silicone foam regulator surfactant are mixed with 35 parts by weight of MDI thereby producing a rigid, fine cells, polyurethane foam which weighed about 1 lb./cu. ft. After 1 week a ½″×2″×6″ vertically placed sample of this foam was tested using a 2″ blue Bunsen burner flame placed at the bottom of the sample for 1 minute. The foam under the flame formed a char. The foam did not catch on fire.

Example 14

Example 1 is modified wherein the aqueous urea is heat to the boiling point of the solution thereby producing an aqueous urea condensate then reacted with the sulfuric acid. Aqueous ammonia is added until the desirable pH is obtained.

Example 15

Example 13 is modified wherein 20 parts by weight of a carbonization auxiliary is added to 100 parts by weight of the aqueous ammonium urea condensate salt of sulfuric acid containing 30% ammonium urea condensate salt of sulfuric acid thereby producing an aqueous ammonium urea condensate salt of sulfuric acid composition and the carbonization auxiliary is selected from the list below:

a) dimelamine phosphate

b) dicyandiamide phosphate

c) urea dihydrogen phosphate

d) guanidine phosphate

e) aminoguanidine phosphate

f) diethyltriamine urea phosphate

g) melamine salt of dimethyl methyl phosphonate

h) melamine salt of dimethyl hydrogen phosphite phosphite

i) methylamine melamine phosphoric acid

j) methyl carbamate salt of phosphoric acid phosphate

k) melamine salt of boron-hydrogen phosphate

l) O-methyl urea

m) urea salt of boron-phosphate

n) urea-formaldehyde phosphate

o) aminophenol phosphate

p) ammonium urea phosphate

q) ammonium melamine phosphate

r) melamine salt of trimethyl

s) melamine salt of phenyl acid

t) ammonium sulfate

Example 16

Example 14 is modified wherein 10 parts by weight of a filler selected from the list below is added to the aqueous ammonium urea condensate salt of sulfuric acid:

a) hydrated aluminum oxide powder

b) hydrated sodium silicate powder

c) melamine

d) dicyandiamide

e) urea sulfate

f) melamine phosphate

g) melamine borate

h) ammonium phosphate

i) ammonium pyrophosphate

j) ammonium carbonate

k) ammonium borate

l) ammonium sulfamate

m) guanidine

n) guanidine carbonate

o) urea phosphate

p) silica powder

q) phenol-formaldehyde resin powder

r) aluminum phosphate

s) thiourea

t) hollow beads

u) expandable graphite

v) melamine salt of DMMP

r) ammonium sulfate

s) magnesium chloride

t) antimony trioxide

u) boron-phosphate powder

v) melamine boron-phosphate powder

w) lignin

x) lignin sulfate

Example 17

Example 10 is modified wherein 10 parts by weight of a phosphorus salt forming compound is added to the aqueous ammonium urea condensate salt of sulfuric acid and selected from the list below:

a) phosphoric acid

b) pyrophosphoric acid

c) dimethyl methyl phosphonate (DMMP)

d) dimethyl hydrogen phosphite

e) trimethyl phosphite

f) phenyl acid phosphate

g) phosphorus trichloride

h) phosphinic acid

i) phosphorus oxytrichloride

j) ammonium dihydrogen phosphate

k) dimethyl phosphoric acid

l) diethyl ethyl phosphonate

m) magnesium hydrogen phosphate

n) mono aluminum phosphate

Example 18

100 parts by weight of the aqueous nitrogen containing compound urea condensate salt of sulfuric acid of claim 1 are mixed with 25 parts by weight of a halogenated flame retardant compound thereby producing an aqueous nitrogen containing compound urea condensate salt of sulfuric acid composition, and the halogenated flame retardant compound is selected from the list thereby producing a flame retardant composition:

a) brominated epoxy olgmer

b) decabromodiphenyl oxide

c) pentabromodiphenyl oxide

d) 2,3-dibromopropanol

e) octabromodiphenyl oxide

f) tris (dichloropropyl) phosphite

g) tris(dichloropropyl) phosphite

Example 19

30 parts by weight of the ammonium urea condensate salt of sulfuric acid of example 2 are mixed and reacted with 15 parts by weight of dimethyl methyl phosphonate (DMMP) thereby producing an ammonium urea condensate salt of sulfuric acid composition, then it was added and mixed with 150 parts by weight of a flexible polyepoxy resins with its polyamine curing agent. The resin is cured then was tested with a 2″ propane flame held against the sample for 1 minute. The flame did not spread and the flame went out when the torch was removed. There was about a 2% weight loss.

Example 20

20 parts by weight of powdered melamine urea condensate salt of sulfuric acid and 5 parts by weight of dimethyl hydrogen phosphite and 5 parts by weight of melamine are incorporated into 70 parts by weight of a flexible polyurethane foam produced from MDI and a triol which weighs about 1.75 lbs./cu.ft. The foam was flame tested by using Calif. 133 Test wherein 100 gms of wood is burned on top of the foam. After burning the wood on the foam there was a 50.5 gms weight loss. A weight loss of less than 60 gms is necessary to pass the test. This foam was flame tested using a ½″×2″×6″ sample hung vertically, then a 2″ propane torch flame was placed at the bottom of the sample for 1 minute. The flame did not spread and the foam melted without burning.

Example 21

30 parts by weight of the powdered ammonium urea condensate salt of sulfuric acid, of example 2, are incorporated in 100 parts by weight of a rigid polyurethane foam of about 1 lbs./cu.ft., produced using polymeric MDI and aromatic polyester polyol. The rigid polyurethane foam was flame tested using a Bunsen burner that had a 2″ flame held against the foam. The flame did not spread and went out when the burner was removed. There was about a 4% weight loss.

Example 22

Example 21 is modified wherein 5 parts by weight of a carbonization agent is added to the powdered ammonium urea condensate salt of sulfuric acid and selected from the list below:

a) dimelamine phosphate

b) dicyandiamide phosphate

c) urea dihydrogen phosphate

d) guanidine phosphate

e) aminoguanidine phosphate

f) diethyltriamine urea phosphate

g) melamine salt of dimethyl methyl phosphonate

h) melamine salt of dimethyl hydrogen phosphite phosphite

i) methylamine melamine phosphoric acid

j) methyl carbamate salt of phosphoric acid phosphate

k) melamine salt of boron-hydrogen phosphate

l) O-methyl urea

m) urea salt of boron-phosphate

n) urea-formaldehyde phosphate

o) aminophenol phosphate

p) ammonium urea phosphate

q) ammonium melamine phosphate

r) melamine salt of trimethyl

s) melamine salt of phenyl acid

t) ammonium sulfate

u) lignin phosphate

Example 23

About 25 parts by weight of the powdered ammonium urea condensate salt of sulfuric acid, produced in Example 2, and 15 parts by weight of dimethyl hydrogen phosphite, 100 parts by weight of triol component (Daloflex XES 11870 by ICI of Europe) and 60 parts by weight of diphenymethane-4,4′-diisocyanate (Suprasec 2424 by ICI) were mixed and foamed into a flexible foam of about 1.5 lbs./cu. ft. After the foam cured for 1 week it was flame tested using Calif. TB 133. The foam sample passed this test with a 44 gms weight loss. Europe's UL94 HF-1, HF-2 flame test were done using a 2 cm flame from a propane torch for 1 minute placed under the ½″×2″×6″ sample. This foam passed the test. The sample did not catch on fire and the melted drips did not catch on fire.

Example 24

Example 23 is modified wherein another carbonization auxiliary is used in place of dimethyl hydrogen phosphite and selected from the list below:

a) dimelamine phosphate

b) dicyandiamide phosphate

c) urea dihydrogen phosphate

d) guanidine phosphate

e) aminoguanidine phosphate

f) diethyltriamine urea phosphate

g) urea salt of dimethyl methyl phosphonate

h) melamine salt of dimethyl hydrogen phosphite phosphite

i) methylamine melamine phosphoric acid

j) methyl carbamate salt of phosphoric acid phosphate

k) melamine salt of boron-hydrogen phosphate

l) Melamine DMMP

m) urea salt of boron-phosphate

n) urea-formaldehyde phosphate

o) aminophenol phosphate

p) ammonium urea phosphate

q) ammonium melamine phosphate

r) melamine salt of trimethyl

s) melamine salt of phenyl acid

t) ammonium sulfate

u) urea condensate phosphate

Example 25

75 parts by weight of aqueous ammonium urea condensate salt of sulfuric acid, produced in example 1,200 parts by weight of sucrose amine polyol, hydroxyl No. 350, 30 parts by weight of ammonium urea phosphate, 0.1 part by weight of amine catalyst (Dabco R8020 by Air Products), 0.5 parts by weight of tin catalyst (Dabco T-12 by Air Products) and 220 parts by weight of Diphenymethane-4,4′-diisocyanate are mixed then poured into a mold. A rigid foam of about 1.5 lbs./cu. ft. is formed. After 1 week this foam is flame tested with a 2″ propane flame by placing the flame at the bottom of a ½″×2″×6″ sample for 1 minute. The flame did not spread and the flame went out when the flame was removed. A char was formed and there was about a 4% weight loss.

Example 26

Example 25 is modified wherein another polyol is used in place of the sucrose amine polyol and selected from the list below:

a) sucrose amine polyol, hydroxyl No. 530 with 25% polypropylene polyol, hydroxyl No. 450;

b) aromatic amino polyol, hydroxyl No. 530 with 25% polypropylene polyol, hydroxyl No. 650;

c) aromatic polyester polyol, hydroxyl No. 350;

d) sucrose polyol, hydroxyl No. 450;

e) phosphorus polyol (VIRCOL 82 by Albright and Wilson).

These samples were tested as above with same good results.

Example 27

Example 25 is modified wherein another polyisocyanate is used and selected from the list below:

a) polymeric MDI (Mondur MR by Miles)

b) polymeric MDI (PAPI 27 by Dow)

c) polymeric MDI (Mondur MRS).

Example 28

100 parts by weight of ethylene modified polypropylene glycol (Multranol 7056 by Miles), 20 parts by weight of the aqueous ammonium urea condensate salt of sulfuric acid example 1, 20 parts by weight of melamine phosphate, 1 part by weight of silicone surfactant (L6202 by Union Carbide), 1 part weight of urethane catalyst and 50 parts by weight of TDI (Mondur TD80) are mixed then poured into a mold. A flame retardant flexible foam of about 1.5 lbs./cu.ft.is produced. The foam was cured for 1 week then flame tested with a 2″ propane flame placed under a ½″×2″×6″ sample (UL94-1,HF-2 TEST). The flame did not spread and the melted drippings did not burn.

Example 29

Example 28 is modified wherein another carbonization agent is added to in place of melamine phosphate and selected from the list below:

a) diaminophosphate

b) dimethyl methyl phosphonate

c) urea phosphate

d) melamine borate

e) ammonium melamine boron phosphate

f) diethyl phosphite

g) ammonium polyphosphate

h) dicyandimide phosphate

i) ammonium phosphate

j) aluminum phosphate

k) tris2-chloroethyl phosphite

l) zinc borate

m) boron oxide

n) boron acid

o) dimethyl phosphite

p) triethy phosphate

q) guanidine phosphate

r) ammonium sulfamate

These examples were tested as in Example 28 and passed this test.

Example 30

30 parts by weight of the aqueous ammonium urea condensate salt of sulfuric acid as produced in Example 1 and 100 parts by weight an aqueous emulsion containing 50% vinyl acetate were mixed then poured into a mold to form a ⅛″ thick sample. After the sample was thoroughly dried the sample was flamed tested by using a 2″ propane flame held against it for 1 minute. The flame did not spread and went out when the flame was removed.

Example 31

Example 30 is modified wherein 10 parts by weight of a carbonization auxiliary is added to the aqueous urea and selected from the list below:

a) dimelamine phosphate

b) dicyandiamide phosphate

c) urea dihydrogen phosphate

d) guanidine phosphate

e) aminoguanidine phosphate

f) diethyltriamine urea phosphate

g) melamine salt of dimethyl methyl phosphonate

h) melamine salt of dimethyl hydrogen phosphite phosphite

i) methylamine melamine phosphoric acid

j) methyl carbamate salt of phosphoric acid phosphate

k) melamine salt of boron-hydrogen phosphate

l) urea melamine phosphate

m) urea salt of boron-phosphate

n) urea-formaldehyde phosphate

o) aminophenol phosphate

p) ammonium urea phosphate

q) ammonium melamine phosphate

r) melamine salt of trimethyl

s) melamine salt of phenyl acid

u) cyanuric phosphate

Example 32

Example 30 is modified wherein the vinyl acetate emulsion is replaced with another emulsion containing 50% by weight of a plastic or natural products listed below;

a) vinyl acetate-ethylene copolymer (Airflex RP-226 by Air Products)

b) vinyl acetate-ethylene copolymer (Airflex RP-245 by Air Products)

c) phenol-formaldehyde resin

d) acrylic enamel paint

e) acrylic latex paint

f) methyl methyl acrylate

g) acrylic acid

h) polyurethane

i) polyester resin

j) epoxy resin

k) starch

l) modified starch

m) polyvinyl chloride

n) polyvinyl chloride-vinyl acetate copolymer

o) polystyrene

p) polyamide from vegetable protein

q) nylon

r) rubber latex

s) polybutadiene-styrene copolymer

These samples were tested as in example 39 and gave the same good results.

Example 33

Example 30 is modified wherein the aqueous emulsion is replaced with an organic solvent containing a solution or emulsion of the plastic or natural product listed in Example 30 and 32 then flame tested. These samples were tested as in Example 29 and gave the good flame retardant results.

Example 34

30 parts by weight of aqueous ammonium urea condensate salt of sulfuric acid produced in Example 1 and 10% cyclic phosphonate (ANTIBLAZE N from Albright & Wilson), are added to an aqueous emulsion of 100 parts by weight of styrene monomer, then a catalytic amount of potassium persulfate and ferric sulfate is added. The mixture is agitated for several hours until the styrene polymerizes. The aqueous emulsion of flame retardant polystyrene is poured into mold and allowed to dry. The dried plastic is then flame tested utilizing a 2″ propane flame which is placed under and touch the plastic for three 10 seconds periods. The flame did not spread and did not bum when the flame was removed.

Example 35

Example 34 is modified wherein another plastic monomer is utilized in place of styrene monomer and selected from the list below:

a) acrylic acid monomer

b) methyl acrylic acid monomer with redox system

c) vinyl acetate monomer

d) vinyl chloride monomer with redox system

e) vinylidene chloride monomer with redox system

f) methyl acrylate monomer with redox system.

g) acrylonitrile monomer with redox system

h) isoprene monomer

i) chloroprene monomer

j) butadiene with acrylonitrile

k) butadiene with styrene

l) N-vinyl pyrrolidone monomer with hydrogen peroxide

m) polyvinyl pyridine monomer

n) vinylidene chloride with vinyl chloride

These samples were tested as in example 33 with the same good results

Example 36

Example 34 is modified wherein 10 parts by weight of titanium oxide is added to reflect heat.

Example 37

Example 34 is modified wherein 3 parts by weight of a carbonization accelerator is added with the aqueous ammonium urea condensate salt of sulfuric acid and selected from the list below:

a) zinc borate

b) zinc oxide

c) calcium magnesium borate

Example 38

Example 34 is modified wherein 5 parts by weight of a filler is added to the aqueous ammonium urea condensate salt of sulfuric acid and selected from the list below:

a) hydrated aluminum oxide powder

b) hydrated sodium silicate powder

c) melamine

d) dicyandiamide

e) urea

f) melamine phosphate

g) melamine borate

h) ammonium phosphate

i) ammonium pyrophosphate

j) ammonium carbonate

k) ammonium borate

l) ammonium sulfamate

m) guanidine

n) guanidine carbonate

o) urea phosphate

p) silica powder

q) phenol-formaldehyde resin powder

r) aluminum phosphate

s) thiourea

t) hollow beads

u) expandable graphite

v) melamine salt of DMMP

r) ammonium sulfate

s) magnesium chloride

t) antimony trioxide

u) boron-phosphate powder

w) melamine boron-phosphate powder

x) ammonium boron-phosphate

y) lignin

Example 39

Example 1 and 2 are modified wherein one mol of a nitrogen containing compound is added to the urea and selected from the list below:

a) melamine

b) ethylene diamine

c) ethanolamine

d) guanidine

e) biuret

f) cyanuric acid

g) ethyl amine

h) urea borate

i) ammonium carbonate

j) ammonium sulfamate

k) ammonium sulfate

l) urea phosphate

m) polyamide with free NH₂— radicals

n) ethylenetriamine

o) polyisocyanate

p) thiourea

Example 40

100 parts by weight of sulfuric acid is reacted with aqueous ammonia to produce ammonium sulfate the 200 parts by weight of urea is added and reacted for 4 hours thereby producing ammonium urea condensate salt of sulfuric acid.

Example 41

200 parts by weight of water containing 50% urea, 20 parts by weight water containing 25% ammonia are mixed then 50 parts by weight of concentrated sulfuric acid is slowly added and reacted thereby producing ammonium urea condensate salt of sulfuric acid, The reaction is exothermic.

Example 42

Example 40 is modified wherein the mixture is heated at 100° C. for 15 minutes.

Example 43

10 parts by weight of a nitrogen containing compound selected from the list below, 100 parts by weight of powdered urea and 30 parts by weight of concentrated sulfuric acid are mixed and reacted thereby producing nitrogen containing compound urea condensate salt of sulfuric acid. The reaction is exothermic and the heat condensates the urea.

a) melamine

b) ammonium carbonate

b) dicyandiamide

c) melamine

d) ammonium sulfate

e) methyl amine

f) ethanolamine

g) diethanolamine

h) ethylene diamine

i) biuret

j) urea carbonate

k) ammonium hydrogen sulfate

l) ammonia borate

m) urea borate

n) diammonium phosphate

o) dicyandiamide

p) thiourea

q) ammonium acetate

r) veramid

s) ammonium carbamate

t) hexamethylene diisocyanate

u) toluene diamine

v) tolylene dissocyanate

w) triethanolamine

x) aniline

y) acetomide

z) aqueous ammonia

Example 44

Example 30 is modified wherein another nitrogen contain compound selected from the group in example 43 and used in place of the aqueous ammonia.

Example 45

Example 2 is modified wherein another sulfur oxyacid and/or sulfur oxyacid salt is used in place of sulfuric acid and selected from this group consisting of sulfurous acid, pyrosulfuric acid, ammonium sulfate, ammonium hydrogen sulfate, ammonium sulfite, ammonium thiosulfate, urea hydrogen sulfate, urea sulfate, melamine hydrogen sulfate, amino hydrogen sulfates, biuret sulfate, lignin sulfate, lignin sulfite, amine hydrogen sulfates, polyamine hydrogen sulfates, alkyl alcohol amines hydrogen sulfates, metal hydrogen sulfates, alkyl hydrogen sulfates, aryl hydrogen sulfates and mixtures thereof.

Example 46

15 parts by weight of ammonium urea condensate of sulfuric produced in Example 43 k and 85 parts by weight of thermoplastic selected from the list below was melted and mixed together. The thermoplastic plastic is selected from the group consisting of vinyl acetate, polyester, polyamide, vinyl chloride, polyethylene, polypropylene and vinyl acetate-ethylene copolymer.

CONCLUSION

Aqueous or powdered nitrogen containing compound urea condensate salt of sulfur oxyacid with or without carbonization auxiliaries greatly increase their flame retardant properties. The addition of other carbonization agents increases the development of an insulating carbon char which helps the materials to resist further degradation and thereby further exposure to flame. A plastic foam for example which contains aqueous or powder nitrogen containing compound urea condensate salt of sulfur oxyacid and/or it's composition, the melted drippings of the material being flame tested is reduced, and any burning and smoke are minimized. There is a lesser amount of smoke given off these flame retardant material when flame tested.

The aqueous ammonium urea condensates salt of sulfur oxyacid or it's composition are inexpensive and are very good flame retardants in fighting grass and forest fires. In fighting forest fires other useful additives may be added such as coloring material, such as ferric oxide, clay, surfactants, anti-corrosive agents, such ammonium phosphates, etc.

It will be appreciated by those skilled in the Arts that changes and modifications of the preferred embodiment can be made without departing from the spirit and broader aspects of the invention as set forth in the appended claims. 

I claim:
 1. A method for reducing combustibility of a more flammable organic material comprising incorporating an aqueous or solid urea condensate salt of sulfur oxyacid and/or aqueous or solid urea condensate salt of sulfur oxyacid composition on or in the more flammable material, under reaction conditions of the more flammable organic material, said aqueous or solid urea condensate salt of sulfur oxyacid and/or composition produced by the method comprising of mixing, heating and reacting the following components: (A) urea condensate, in the amount of 25 to 200 parts by weight of urea condensate; (B) sulfur oxyacid and/or sulfur oxyacid salts that will react with urea, in the amount of 5 to 50 parts by weight of sulfur oxyacid and/or sulfur oxyacid salts; then add and mix (C) metal containing compound that accelerates carbonization, in the amount of 0 to 30 parts by weight of metal containing compound; (D) heat reflecting compound, in the amount of 0 to 30 parts by weight of heat reflecting compound; (E) filler, in the amount of 0 to 300 parts by weight of filler; (F) surfactant that assist in the formation of bubbles, in the amount of 0 to 30 part by weight of surfactant; (G) water, in the amount of 0 to 500 parts by weight of water.
 2. The method of claim 1 wherein the metal containing compound that accelerates carbonization is selected from the group consisting of zinc oxide, zinc thiocarbamate compounds, mercaptobenzothiazole zinc compounds, salicyaldehyde zinc compounds, zinc borate, alkaline earth metal borates and mixtures thereof, in an amount of 0 to 30 parts by weight of said metal compound.
 3. The method of claim 1 where in the surfactant that promotes the formation of bubbles are selected from the group consisting of cationic, anionic, non-ionic and amphoteric surfactants.
 4. The method of claim 1 wherein the flammable organic material is selected from the group consisting of polyurethanes, polyester resins, unsaturated polyester resins, polyepoxy resins, polycarbonates, polyamides, polyimides, polyester-polyamide resins, polyacrylonitrile, vinyl polymers and copolymers, olefin polymers and copolymers, vinyl-olefin copolymers, polyphenylene, polysulfone, polyacetal, and other plastics, natural products and mixtures thereof.
 5. The product produced by the method of claim
 1. 6. The method of claim 1 wherein the sulfur oxyacid and salts which will react with urea condensate is selected from the group consisting of sulfuric acid, sulfurous acid, pyrosulfuric acid, urea hydrogen sulfate, urea sulfate, melamine hydrogen sulfate, amino hydrogen sulfates, biuret sulfate, lignin sulfate, lignin sulfite, amine hydrogen sulfates, polyamine hydrogen sulfates, alkyl alcohol amines hydrogen sulfates, metal hydrogen sulfates, alkyl hydrogen sulfates, aryl hydrogen sulfates and mixtures thereof.
 7. A flame retardant composition produced by applying on and/or incorporating a flame retardant aqueous or solid urea condensate salt of sulfur oxyacid and/or aqueous or solid urea condensate salt of sulfur oxyacid composition in a more flammable organic material, under reaction conditions or applying sufficient amount to reduce the combustibility of the more flammable organic material said aqueous or solid urea condensate salt of sulfur oxyacid or composition is produced by the process consisting of mixing and reacting the following components: A) urea condensate, in the amount of 25 to 200 parts by weight of urea condensate; B) sulfur oxyacid and/or a non-ammonium salts of sulfur oxyacids that will react with urea condensate, in the amount of 5 to 50 parts by weight of sulfur oxyacid and/or salts of sulfur oxyacids; C) metal containing compounds that will accelerate the carbonization process, in the amount of 0 to 30 parts by weight of metal containing compounds; D) heat reflecting material, in the amount of 0 to 30 parts by weight of heat reflecting material; E) surfactant that assists in the formation of bubbles, in the amount 0 to 30 parts by weight of the surfactant; F) filler, in the amount of 0 to 300 parts by weight of filler; G) water, in the amount of 0 to 500 parts by weight of water.
 8. The flame retardant composition of claim 7 wherein urea condensate salt of sulfur oxyacid composition is an aqueous or solid urea condensate salt of sulfuric acid.
 9. The flame retardant composition of claim 7 wherein the flammable organic material is natural products and the flame retardant aqueous urea condensate salt of sulfur oxyacid is applied on the natural products.
 10. The flame retardant composition of claim 7 wherein the aqueous urea condensate salt of sulfur oxyacid is applied on a burning organic material.
 11. The flame retardant composition of claim 7 wherein the metal containing compound that accelerates the carbonization is selected from the group consisting of zinc oxide, zinc thiocarbamate compounds, mercaptobenzothiazole zinc compounds, salicyaldehyde zinc compounds, zinc borate, alkaline earth metal borates and mixtures thereof.
 12. The flame retardant composition of claim 7 wherein the heat reflecting substance is titanium oxide.
 13. The flame retardant composition of claim 7 wherein the more flammable organic material is selected from the group consisting of polyurethanes, polyester resins, unsaturated polyester resins, polyepoxy resins, polycarbonates, polyamides, polyimides, polyester-polyamide resins, polyacrylonitrile, vinyl polymers and copolymers, olefin polymers and copolymers, vinyl-olefin copolymers, polyphenylene, polysulfone, polyacetal, and other plastics,natural products and mixtures thereof.
 14. A flame retardant composition of claim 1 wherein the urea condensate salt of sulfur oxyacid is produced by heating and reacting urea condensate with sulfuric acid thereby producing a urea condensate salt of sulfuric acid. 